GMP Bridge AG
Managing Consultant
I am a senior Quality and GMP advisor with 18 years of experience across biopharma, biologics, ATMPs, and CDMO environments. My career spans sterile manufacturing operations, corporate Quality leadership, and complex regulatory transitions, from clinical development through commercial readiness, working with both global organizations and clinical-stage biotechs across Europe, North America, and Asia.
I am the Founder and Managing Director of GMP Bridge AG, a senior consulting firm headquartered in Basel, Switzerland, specializing in inspection readiness, contamination control, CDMO oversight, and Quality system transformation for biopharma and advanced therapy companies.
With over 250 GxP audits conducted globally and more than 25 regulatory inspections supported with FDA, EMA, Swissmedic, and ANVISA, I bring the depth of experience that complex GMP challenges require: strategic thinking grounded in operational reality.
Within ISPE, I am an active member of the Nordics Affiliate and serve as Chair of the Community of Practice for Quality. I am committed to advancing practical, risk-based approaches to GMP compliance and to building a stronger community of senior Quality professionals across the industry.